QC Analyst

Overview The QC Analyst will execute laboratory testing and quality control activities within a GMP-regulated pharmaceutical manufacturing environment. The role ensures accurate analytical testing, proper sample management, equipment support, and full compliance with cGxP and data integrity standards. Key Responsibilities Perform analytical testing of API, drug substance, drug product, finished product, stability and packaging material samples Manage sample storage, handling, and documentation Ensure accurate and timely GMP-compliant documentation Support equipment maintenance, calibration, and qualification activities Maintain inspection readiness and adhere to SOPs, GMP, and HSE standards Participate in training, retraining, and continuous improvement initiatives Requirements & Qualifications Experience Prior experience in pharmaceutical QC laboratory environment Hands-on analytical testing experience Exposure to GMP documentation and data integrity practices Aseptic technique experience Education Diploma / Apprenticeship as Laboratory Assistant or equivalent technical qualification Technical Knowledge QC testing and sampling Knowledge of GMP/GxP standards Familiarity with laboratory equipment and quality systems Skills & Competencies Detail-oriented and compliance-driven Strong documentation discipline Team-oriented and result-focused Able to work 12-hour rotating shifts